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A small molecule CFTR potentiator restores ATP-dependent channel gating to the cystic fibrosis mutant G551D-CFTR.

Jia LiuAllison P BergYiting WangWalailak JantarajitKaty J SutcliffeEdward B StevensLishuang CaoMarko J PregelDavid N Sheppard
Published in: British journal of pharmacology (2021)
CP-628006 has distinct effects compared to ivacaftor, suggesting a different mechanism of CFTR potentiation. The emergence of CFTR potentiators with diverse modes of action makes therapy with combinations of potentiators a possibility.
Keyphrases
  • cystic fibrosis
  • pseudomonas aeruginosa
  • small molecule
  • lung function
  • stem cells
  • chronic obstructive pulmonary disease
  • bone marrow
  • wild type